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1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER

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1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER Basic information

Product Name:
1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER
Synonyms:
  • 1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER
  • 1, 1-ACCB(OME)
  • Cyclobutanecarboxylic acid, 1-amino-, methyl ester (9CI)
  • Cyclobutanecarboxylic acid, 1-aMino-, Methyl ester
  • Methyl 1-aMinocyclobutanecarboxylate
  • methyl 1-aminocyclobutane-1-carboxylate
  • 1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER USP/EP/BP
  • Cyclobutanecarboxylicacid, 1-amino-, methyl ester, hydrochlo...
CAS:
215597-35-6
MF:
C6H11NO2
MW:
129.16
Product Categories:
  • AMINEPRIMARY
  • AMINOACID
  • pharmacetical
Mol File:
215597-35-6.mol
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1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER Chemical Properties

Boiling point:
162.3±23.0 °C(Predicted)
Density 
1.127±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
pka
7.71±0.20(Predicted)
form 
Solid
Appearance
Colorless to light yellow Liquid
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
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1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER Usage And Synthesis

Synthesis

67-56-1

120728-10-1

215597-35-6

Stage 1: Synthesis of methyl 1-aminocyclobutanecarboxylate Concentrated H2SO4 (10 ml) was slowly added to a methanol solution (30 ml) containing 1-(tert-butoxycarbonylamino)-cyclobutane-1-carboxylic acid (9.29 mmol, 1 eq.) at 0°C. The reaction mixture was refluxed at 0°C for 2 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was dissolved in distilled water and the pH was adjusted to 8-9 with saturated sodium bicarbonate solution, followed by extraction with ethyl acetate (2 x 200 ml). The combined organic phases were washed sequentially with distilled water (2 x 150 ml) and saturated NaCl solution (2 x 50 ml) and dried with anhydrous sodium sulfate. Finally, the solvent was removed by concentration under reduced pressure to afford methyl 1-aminocyclobutanecarboxylate as a white solid in 75% yield.

References

[1] Patent: US2010/173889, 2010, A1. Location in patent: Page/Page column 34

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